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小粒径同质/异质壳层结构NaGdF4:3%Nd3+纳米颗粒的近红外发光特性 被引量:1
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作者 马文君 由芳田 +1 位作者 彭洪尚 黄世华 《物理学报》 SCIE EI CAS CSCD 北大核心 2017年第10期296-301,共6页
采用共沉淀法制备了粒径小于5 nm的六方相NaGdF_4:3%Nd^(3+)纳米颗粒.纳米颗粒表面缺陷会使发光中心产生严重的淬灭,对其表面包覆适当厚度的壳层可以有效地减少发光淬灭,提高发光性能.对NaGdF_4:3%Nd^(3+)核心纳米颗粒分别进行同质和异... 采用共沉淀法制备了粒径小于5 nm的六方相NaGdF_4:3%Nd^(3+)纳米颗粒.纳米颗粒表面缺陷会使发光中心产生严重的淬灭,对其表面包覆适当厚度的壳层可以有效地减少发光淬灭,提高发光性能.对NaGdF_4:3%Nd^(3+)核心纳米颗粒分别进行同质和异质包覆并且通过调节核壳比制备了不同壳层厚度的NaGdF_4:3%Nd^(3+)@NaGdF_4和NaGdF_4:3%Nd^(3+)@Na YF4纳米颗粒,研究了不同的壳层厚度对核心纳米颗粒发光的影响,并对两种不同核壳结构纳米颗粒的发光性能进行了对比.在808 nm近红外光激发下,NaGdF_4:3%Nd^(3+)纳米颗粒发射出位于约866,893,1060 nm的近红外发射.与核心纳米颗粒相比,核壳结构的纳米颗粒的荧光强度增强,荧光寿命增长,并且随着壳厚的增加,荧光强度出现先增强后减弱、荧光寿命逐步增长的趋势.与相同条件下同质包覆的NaGdF_4:3%Nd^(3+)@NaGdF_4纳米颗粒相比,异质包覆的NaGdF_4:3%Nd^(3+)@NaYF_4纳米颗粒光谱荧光强度增强,寿命增长. 展开更多
关键词 近红外发光 同质结构 异质核壳结构 NaGdF4:Nd3+
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CdSe包覆层数对水溶性CdTe/CdSe(Ⅱ型)核壳量子点的光学特性和微观结构的影响 被引量:5
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作者 彭静 方晓明 +1 位作者 陈志鸿 张正国 《物理化学学报》 SCIE CAS CSCD 北大核心 2012年第1期232-238,共7页
在水相合成的CdTe量子点的体系中通过分批次加入新鲜配制的NaHSe和CdCl2溶液,制备出了CdSe包覆层数不同的CdTe/CdSe核壳量子点,并着重考察了CdSe包覆层数对CdTe/CdSe核壳量子点的光学特性以及微观结构的影响.与CdTe量子点相比,CdSe单层... 在水相合成的CdTe量子点的体系中通过分批次加入新鲜配制的NaHSe和CdCl2溶液,制备出了CdSe包覆层数不同的CdTe/CdSe核壳量子点,并着重考察了CdSe包覆层数对CdTe/CdSe核壳量子点的光学特性以及微观结构的影响.与CdTe量子点相比,CdSe单层包覆的CdTe/CdSe核壳量子点的吸收峰和荧光发射峰出现明显红移;随着CdSe包覆层数的增多,CdTe/CdSe核壳量子点吸收光谱的覆盖范围向长波方向扩展,荧光发射峰强度逐步下降,荧光寿命大幅延长,体现出Ⅱ型核壳量子点的特征.X射线衍射(XRD)分析表明,随着CdSe包覆层数的增多,CdTe/CdSe核壳量子点的粉末衍射峰由CdTe衍射峰位置逐步向CdSe衍射峰位置靠近.CdTe/CdSe核壳量子点因其延伸到近红外区域的宽吸收特性致使其在太阳电池领域具有重要的应用前景. 展开更多
关键词 量子点 Ⅱ型异质结构 CdTe/CdSe 水相合成
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P掺杂Co_(9)S_(8)@VS_(2)纳米管阵列的制备及其水性锌离子混合超级电容器性能研究 被引量:2
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作者 张浩 刘梦洁 +1 位作者 钱惠 张惠 《功能材料》 CAS CSCD 北大核心 2022年第3期3136-3145,共10页
近年来,二硫化钒(VS_(2))作为一种具有二维层状结构的高表面活性的过渡金属硫化物而广泛地应用在锌离子电池(ZIBs)正极材料中。然而,VS_(2)的生长堆叠问题和低能量密度严重阻碍了其在储能设备中的应用。通过在Co_(9)S_(8)纳米管阵列(NT... 近年来,二硫化钒(VS_(2))作为一种具有二维层状结构的高表面活性的过渡金属硫化物而广泛地应用在锌离子电池(ZIBs)正极材料中。然而,VS_(2)的生长堆叠问题和低能量密度严重阻碍了其在储能设备中的应用。通过在Co_(9)S_(8)纳米管阵列(NTAs)表面包覆生长P掺杂VS_(2)纳米片的方式构建一种具有核壳异质结构的Co_(9)S_(8)@P-VS_(2) NTAs,从而有效地避免了大块VS_(2)纳米片的堆积生长,使得层状VS_(2)被分散包覆在纳米管的表面;而且P掺杂增强了Co_(9)S_(8)纳米管与VS_(2)纳米之间异质结的导电性,提升了其比容量,进而提高了能量密度。因此,得益于纳米核壳结构与P掺杂改性的协同作用,制备的Co_(9)S_(8)@P-VS_(2) NTAs在作为电容型正极与电池型锌负极组装成新型的锌离子混合超级电容器(ZHSCs)后获得了优异的电化学储能性能。前驱液中的磷源加入量为30μL/35 mL,2 mol/L ZnSO_(4)水系电解质中,Co_(9)S_(8)@P-VS_(2) NTAs(Co_(9)S_(8)@P-VS_(2)-30 NTAs)获得了一个高达6.72 F/cm^(2)的超高面积比电容(电流密度:2 mA/cm^(2)),远高于Co_(9)S_(8)@VS_(2) NTAs(2.98 F/cm^(2));在1.6 W/cm^(2)的功率密度下,其能量密度可以达到2.39 mWh/cm^(2);并且在1000个循环充放电后,其面积比容量仍能保持为初始比电容的74.26%,具有良好的循环稳定性。 展开更多
关键词 VS_(2) Co_(9)S_(8) P掺杂 过渡金属硫化物 异质结构 锌离子混合超级电容器
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One-pot hydrothermal synthesis of willow branch-shaped MoS_2/CdS heterojunctions for photocatalytic H_2 production under visible light irradiation 被引量:12
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作者 Zhen-Wei Zhang Qiu-Hao Li +2 位作者 Xiu-Qing Qiao Dongfang Hou Dong-Sheng Li 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第3期371-379,共9页
Willow branch-shaped MoS2/CdS heterojunctions are successfully synthesized for the first time by a facile one-pot hydrothermal method. The as-prepared samples were characterized by X-ray diffraction, X-ray photoelectr... Willow branch-shaped MoS2/CdS heterojunctions are successfully synthesized for the first time by a facile one-pot hydrothermal method. The as-prepared samples were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, nitrogen adsorption-desorption measurements, diffuse reflectance spectroscopy, and photoelectrochemical and photoluminescence spectroscopy tests. The photocatalytic hydrogen evolution activities of the samples were evaluated under visible light irradiation. The resulting MoS2/CdS heterojunctions exhibit a much improved photocatalytic hydrogen evolution activity than that obtained with CdS and MoS2. In particular, the optimized MC-5 (5 at.% MoS2/CdS) photocatalyst achieved the highest hydrogen production rate of 250.8 μmol h–1, which is 28 times higher than that of pristine CdS. The apparent quantum efficiency (AQE) at 420 nm was 3.66%. Further detailed characterizations revealed that the enhanced photocatalytic activity of the MoS2/CdS heterojunctions could be attributed to the efficient transfer and separation of photogenerated charge carriers resulting from the core-shell structure and the close contact between MoS2 nanosheets and CdS single-crystal nanorods, as well as to increased visible light absorption. A tentative mechanism for photocatalytic H2 evolution by MoS2/CdS heterojunctions was proposed. This work will open up new opportunities for developing more efficient photocatalysts for water splitting. 展开更多
关键词 CDS MoS2 Photocatalysis Water splitting H2 evolution HETEROJUNCTION Core-shell structure Visible light
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Visible-light-induced NiCo_(2)O_(4)@Co_(3)O_(4) core/shell heterojunction photocatalysts for efficient removal of organic dyes 被引量:2
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作者 WANG Huan-wei FANG Xin +3 位作者 WAN Yu-chi ZHAN Jing WANG Zhi-jian LIU Hua 《Journal of Central South University》 SCIE EI CAS CSCD 2021年第10期3040-3049,共10页
Semiconductor photocatalysis has been considered as a potential technology for the removal of organic dyes from wastewater.The development of photocatalysts with high stability and strong catalytic activity is the mos... Semiconductor photocatalysis has been considered as a potential technology for the removal of organic dyes from wastewater.The development of photocatalysts with high stability and strong catalytic activity is the most important in application.Visible-light-induced NiCo_(2)O_(4)@Co_(3)O_(4) core/shell heterojunctions were synthesized via a sol-gel method in this paper.Compared to bare NiCo_(2)O_(4) and Co_(3)O_(4),NiCo_(2)O_(4)@Co_(3)O_(4) showed a remarkably enhanced removal rate towards congo red(CR)degradation with 98.4%of the removal rate to CR at 120 min under irradiation.The excellent performance of NiCo_(2)O_(4)@Co_(3)O_(4) benefits from the effective separation of photogenerated electron-holes by forming a heterojunction,and the rapid transfer efficiency of photo-generated charge carriers results from the core/shell architectures.A mechanism that NiCo_(2)O_(4)@Co_(3)O_(4) degrades CR to harmless inorganic substances by h^(+),•O-2 and•OH during the photocatalytic process was proposed. 展开更多
关键词 visible-light-inducment NiCo_(2)O_(4)@Co_(3)O_(4) HETEROJUNCTION core/shell architectures
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烧结时间对Fe-Si/SiO_(2)软磁铁芯微观结构演变及磁性能的影响
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作者 孔辉 王锐 +3 位作者 吴朝阳 贺弋海 王海川 鞠纳川 《过程工程学报》 CAS CSCD 北大核心 2023年第6期898-907,共10页
软磁铁芯由铁基软磁合金粉末和作为绝缘层的氧化物陶瓷组成,这二者在软磁铁芯中形成的核壳异质结构是限制交流磁化过程中涡流运转和降低高频损耗的基础,因此在烧结成型过程中保持软磁铁芯内核壳异质结构的完整性和均匀性对优化其磁性能... 软磁铁芯由铁基软磁合金粉末和作为绝缘层的氧化物陶瓷组成,这二者在软磁铁芯中形成的核壳异质结构是限制交流磁化过程中涡流运转和降低高频损耗的基础,因此在烧结成型过程中保持软磁铁芯内核壳异质结构的完整性和均匀性对优化其磁性能至关重要。本工作制备了Fe-Si/SiO_(2)软磁铁芯,并研究了Fe-Si/SiO_(2)核壳异质结构随烧结时间的演化行为及对软磁铁芯磁性能的影响。结果表明,在3~10 min范围内,随烧结时间的延长Fe-Si/SiO_(2)软磁铁芯内核壳异质结构逐渐趋于完整,烧结时间为9 min时,SiO_(2)绝缘层开始结晶;当烧结时间超过11 min时,由于热压烧结过程中的梯度温度场引起的过热现象,导致核壳异质结构坍塌。在核壳异质结构保持完整的情况下,烧结时间为10 min的Fe-Si/SiO_(2)软磁铁芯性能较佳,饱和磁化强度为220.9 emu/g,电阻率为0.72 mΩ·cm,总损耗Pcv(10 mT,100 kHz)为627.5 kW/m3。相比于核壳异质结构坍塌的样品(13 min),总损耗Pcv(10 mT,100 kHz)降低约38.7%,其中涡流损耗降低了约33.1%,磁滞损耗降低了约14.7%。 展开更多
关键词 烧结时间 异质结构 软磁铁芯 演化行为 磁性能
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流态化气相沉积过程中稀释气体流量对颗粒表面SiO_(2)沉积的影响 被引量:3
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作者 吴朝阳 高子涵 +3 位作者 孔辉 先琛 贾吉祥 廖相巍 《过程工程学报》 CAS CSCD 北大核心 2021年第8期959-968,共10页
利用Fe(Si)合金球形粉末为沉积基底,正硅酸乙酯为SiO_(2)气相介质前驱体,采用引入流化环节的化学气相沉积工艺合成了Fe(Si)/SiO_(2)复合粉末。考察了沉积过程中Ar稀释气体流量对Fe(Si)基底粉末表面SiO_(2)绝缘介质沉积过程的影响规律及... 利用Fe(Si)合金球形粉末为沉积基底,正硅酸乙酯为SiO_(2)气相介质前驱体,采用引入流化环节的化学气相沉积工艺合成了Fe(Si)/SiO_(2)复合粉末。考察了沉积过程中Ar稀释气体流量对Fe(Si)基底粉末表面SiO_(2)绝缘介质沉积过程的影响规律及形成完整核壳异质结构的稀释气体流量范围。实验结果表明,随着流态化气相沉积过程中Ar稀释气体流量的逐渐增大,SiO_(2)绝缘介质在Fe(Si)粉末基底表面的微观形貌从亚微米级团簇转变为完整薄膜再向多孔薄膜转变,沉积速率先减小后增大再降低,在250 sccm时SiO_(2)绝缘介质均匀性最好,沉积速率为0.069 nm/s。此外,形成完整Fe(Si)/SiO_(2)核壳异质结构的Ar稀释气体流量范围为200~300 sccm。 展开更多
关键词 流态化气相沉积 稀释气体流量 异质结构 铁硅合金 结构演化
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Epitaxial growth of hyperbranched Cu/Cu2O/CuO coreshell nanowire heterostructures for lithium-ion batteries 被引量:2
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作者 Yuxin Zhao Ying Zhang +5 位作者 Hu Zhao Xuejin Li Yanpeng Li Ling wen Zifeng Yan Ziyang Huo 《Nano Research》 SCIE EI CAS CSCD 2015年第8期2763-2776,共14页
The careful design of nano-architectures and smart hybridization of expected active materials can lead to more advanced properties. Here we have engineered a novel hierarchical branching Cu/Cu2O/CuO heteronanostructur... The careful design of nano-architectures and smart hybridization of expected active materials can lead to more advanced properties. Here we have engineered a novel hierarchical branching Cu/Cu2O/CuO heteronanostructure by combining a facile hydrothermal method and subsequent controlled oxidation process. The fine structure and epitaxial relationship between the branches and backbone are investigated by high-resolution transmission electron microscopy. Moreover, the evolution of the branch growth has also been observed during the gradual oxidation of the Cu nanowire surface. The experimental results suggest that the surface oxidation needs to be performed via a two-step exposure process to varying humidity in order to achieve optimized formation of a core-shell structured branching architecture. Finally, a proof-of-concept of the function of such a hierarchical framework as the anode material in lithium-ion batteries is demonstrated. The branching core-shell heterostructure improves battery performance by several means: (i) The epitaxially grown branches provide a high surface area for enhanced electrolyte accessibility and high resistance to volume change induced by Li^+ intercalation/extraction; (ii) the core-shell structure with its well-defined heterojunction increases the contact area which facilitates effective charge transport during lithiation; (iii) the copper core acts as a current collector as well as providing structural reinforcement. 展开更多
关键词 nanowires copper oxides epitaxial growth HETEROSTRUCTURE lithium-ion battery
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